Canonical Allele Identifier: CA2580090800
Gene: XYLT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2237790
ClinVar RCV Id: RCV002724196

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138410_17138439dup , CM000678.2:g.17138410_17138439dup GRCh38
NC_000016.9:g.17232267_17232296dup , CM000678.1:g.17232267_17232296dup GRCh37
NC_000016.8:g.17139768_17139797dup NCBI36
NG_015843.1:g.337446_337475dup
NG_015843.2:g.337446_337475dup

Transcript Alleles

HGVS Amino-acid change
ENST00000261381.7:c.1683_1712dup MANE Select ENSP00000261381.6:p.Asp570_Trp571insCysLy...
ENST00000261381.6:c.1683_1712dup ENSP00000261381.6:p.Asp570_Trp571insCysLy...
NM_022166.3:c.1683_1712dup NP_071449.1:p.Asp570_Trp571insCysLysCysGl...
XM_011522574.1:c.1683_1712dup XP_011520876.1:p.Asp570_Trp571insCysLysCy...
XR_933141.1:n.343_372dup
NR_135179.1:n.315_344dup
XM_017023539.2:c.1683_1712dup XP_016879028.1:p.Asp570_Trp571insCysLysCy...
XM_017023540.2:c.1683_1712dup XP_016879029.1:p.Asp570_Trp571insCysLysCy...
NM_022166.4:c.1683_1712dup MANE Select NP_071449.1:p.Asp570_Trp571insCysLysCysGl...